| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA02g47670 | A02 | 38444360 | G | A | missense_variant | MODERATE | c.112G>A|p.Val38Ile |
S292 |